Vaccination

The Vaccine Debate: Insults, Lies, & Hypocrisy

It’s been 10 years since I first delved into the topic of vaccination. With hopes of finding definitive answers, I combed through thousands of studies and articles written by a wide spectrum of authors – some heavily pro, some deeply against, and many in between.

Ten years on I’ve learnt a lot, knowing there is always so much more to learn, but I find myself disillusioned with what should be a straight forward, logical topic. I know many others feel the same. I’ve found I can’t enter into the topic of vaccination without being inundated with insults, lies, and hypocrisy (hence the title of this post).

While I’ve seen people on all sides of this debate guilty of it to varying degrees, the majority of it seems to stem from the staunchly pro-vax camp. I’m not talking about the average parent who feels vaccinating is best for their family, more power to you.

I’m talking about the rabid pro-vaccine advocate who believes they have the right to FORCE each and every one of us  to vaccinate. They believe vaccination is a black and white topic, they believe those who disagree with their opinions are the enemy, and they believe you shouldn’t get to choose what is injected into your own or your children’s bodies.

One thing’s for sure, I’m sick of hearing and seeing it; it needs to end. Here's a taste of what I'm talking about:

People use pictures and stories of sick or dead children to expose the reality of the diseases we vaccinate for, but they downplay or dismiss pictures and stories of children who become sick or die due to vaccine injury, calling them ‘scare tactics’.

It's mind boggling that it has to be said: no death or injury, whatever the cause, should ever be callously disregarded. When parents are told by their family GP, “vaccines are perfectly safe, your child will be fine”, only to have their child injured or die as a result of vaccination, the trauma is particularly painful. The trust they invested in the medical profession is destroyed.

The anguish is made worse when medical professionals refuse to even acknowledge the vaccine they administered was the cause. Instead of being comforted in their time of need, these families feel shunned. Imagine being in that position, hearing people disregard your child's injury or death?

Hear this well: our children’s lives aren’t anyone else's to expend as collateral damage for ‘the greater good’. Those who think they are should be utterly ashamed. No one gets to force anything into us or our children, ever.

People herald parents who speak out about their child’s sickness or death due to the diseases we vaccinate for as brave heroes, but they disbelieve and insult parents who speak out about their child’s sickness or death due to vaccine injury, labelling them ‘liars’, ‘scum’, ‘anti-science’, etc. 

The cruelty in this debate is both heartbreaking and enraging. There is much, much worse said to these parents I won’t mention here [1-3]. Grieving parents of sick or dead children no matter the cause, who speak out in the hopes of saving others the misery they had to endure, deserve a listening ear and a shoulder to cry on;  not insults and ostracism. Any human being should inherently understand this, but somehow this debate turns usually decent people into vicious assholes at the flick of a switch.

Hear this well: no one else gets to tell parents what did or did not happen to their child; we didn't witness it, we don’t know their children. Have some respect.

The above two examples are the two that irk me the most, more so because my own son suffered a severe vaccine reaction. But there’s plenty more…

People call parents who choose not to vaccinate due to fear of adverse reaction ‘uneducated’ and ‘irresponsible’, but these same people choose to vaccinate their own children due to fear of adverse reactions to diseases we vaccinate for.

Fear of injury or death is the common denominator driving the decision to vaccinate or not vaccinate, so if one side is deemed ‘irresponsible’ for letting fear for their children’s lives determine their decision, then so must the other. It boils down to: what poses a greater risk to my child, vaccinating or not vaccinating?

There is a wealth of evidence in support for both. For our family, the experience of brain injury our son suffered after vaccination made it abundantly clear vaccines posed a greater risk than the extremely small risk of disease complications he faced [4-22]. I cannot guarantee another family will not suffer the same fate our family did, or worse, because there is so little recognition of vaccine injury [23-26] or research regarding which children are most susceptible to vaccine injury [27].

In contrast, there has been abundant research regarding who is most susceptible to the diseases we currently vaccinate for. We know what makes people more likely to suffer complications of infectious diseases (eg. poor diet, nutritional deficiencies, immune deficiencies, chronic diseases, multiple simultaneous illnesses, excessive stress, not breastfeeding, smoking, alcohol consumption, exposure to toxins and pollutants, obesity, lack of physical activity, unsanitary or overcrowded living conditions, age very young or very old, etc [28-50]).

People proclaim vaccine injury is extremely rare and not reason enough to avoid vaccination, but they promote extremely rare complications from the diseases we vaccinate for as a reason to vaccinate. 

The fact that vaccine injury is grossly under-reported is ignored [51], along with the fact that doctors often refuse to acknowledge vaccine injury, never mind report it [23-26]. Vaccine injury is often missed or passed off as coincidental by parents and GP’s. When concerned parents ring their doctors office to report their child has a high-pitched, prolonged cry indicating encephalitis – a brain injury that can result in chronic seizures, mental retardation, and death [52-54] - they are told this reaction is normal!

It might be such a common vaccine reaction that today’s medical staff now consider an encephalitic cry ‘normal’, but the reality is encephalitis is a serious, life threatening reaction, often resulting in permanent neurological impairments. I shudder to think how many children whose parents were told their child’s reaction was, “normal and nothing to worry about”, went on to suffer neurological and developmental disorders.

If only these children had been medically tested and treated for encephalitis, just maybe the severity of permanent injury could have been reduced. If only more research was done to determine which children are more susceptible to vaccine injury, maybe the vaccine injury could have been completely avoided altogether.

People claim that there is ‘abundant’ evidence to show that  ‘vaccines are safe’, but they ignore the fact that the vaccine schedule in its entirety, or vaccines in their various combinations, have NEVER been tested for safety [55], nor has there ever been a safety study comparing unvaccinated children with vaccinated children.

The only survey of unvaccinated children with vaccinated children was done by Generation Rescue in 2007 which found that, “vaccinated boys had a 155% greater chance of having a neurological disorder like ADHD or autism than unvaccinated boys”. [56]

People claim to have done ‘extensive scientific research’ on vaccination, but they go on to state the only study linking vaccines to autism was, “that one fraudulent Wakefield study”, and they only share information from biased websites. 

There have been numerous studies since Wakefield associating vaccines with autism, but you won’t find them mentioned on websites whose sole purpose is to promote vaccination [57-77]. We can’t claim to know everything on  a topic by only reading material from one sided sources, in fact we can never claim to know everything on any topic. If there’s one thing I’ve learnt about the vaccination debate it’s that there’s always more to learn and nothing is written in stone. Always be ready to change your mind and be proven wrong.

People promote heavily flawed research funded by pharmaceutical companies, and organisations that have been exposed by their own employees for manipulating data [79-89], but they call any research showing the harms of vaccination ‘junk science’ authored by ‘quacks’. 

Neuroscientist Russell Blaylock is one example of a study author who has found evidence of harm due to vaccines [59]. Because his research was critical of vaccination he is disregarded by many vaccine advocates without any evidence to justify it at all. Unlike many CDC or pharmaceutical industry study authors you won’t find evidence of fraud or twisting of data in Blaylocks research, but for the sake of keeping their beliefs about vaccination intact people pretend researchers like Blaylock aren’t worth listening to.

People present only research that backs their personal opinion, then ignore all other research presented to them that contradicts their own narrow research, dismissing it as nothing more than ‘cherry picked studies’. 

They think their own ‘cherry picked studies’, however, are all they need to form a scientifically sound opinion. Tossing out contradictory evidence to keep their own beliefs intact.

People dismiss research showing a link between vaccines and injury, claiming, “correlation does not equal causation”, but they go on to claim the correlation between vaccination and disease decline is evidence of causation. 

They ignore the fact that historical records show disease rates were already declining when vaccines were introduced, many by more than 90%, due to improved sanitation, nutrition, housing etc [90]. Instead of acknowledging these time-tested methods of disease reduction, they attribute the decline of disease entirely to vaccination! How can a vaccine that wasn't invented yet be responsible for a 90% decline in disease and mortality?

As for vaccine injury, many vaccine injuries are documented by VAERS, with 83% of those reports coming from doctors and pharmaceutical company employees, not the actual victims [90a]. However, VAERS states these reports are greatly under-reported [90a]. We truly don’t know the real number of serious, debilitating, sometimes fatal vaccine reactions that have occurred. Additionally, because pharmaceutical companies refuse to test their vaccines with a proper control population (a group of individuals who only receive a saline injection and has never been vaccinated, compared with a group who receives a vaccine) it becomes more difficult to conclusively pin down vaccines as a cause of injury.

Many people are happy to refute reports of vaccine injury as 'coincidence', but any other report of a drug that someone reacts to is taken much more seriously. Pharmaceutical companies have marketed vaccines so successfully that they seem to be considered by many as untouchable, beyond criticism.

Nobody dares criticize or even hint that vaccines have the ability to cause injury, or they'll be deemed an 'antivaxxer' and an 'enemy of the people' in a very Stalin-esque manner (for the record I am not 'antivax' - the original idea Jenner had for deliberately getting infected with a mild illness to protect yourself from a more severe illness I think is a brilliant one in many respects - I am 'pro-safe-vax').

For those unwilling to change their minds, no amount of evidence will ever be enough to prove causation; for them all evidence that contradicts their beliefs will forever be considered ‘correlation’. 

People promote the use of vaccination to try to prevent disease despite the risk of adverse reaction, but completely ignore other scientifically proven disease prevention methods that don’t carry any risk of adverse reaction.

These include healthier diets, monitoring and correction of nutritional deficiencies, reducing exposure to toxins and pollutants, reducing stress, reducing poverty, unsanitary living conditions, and overcrowding in homes, higher breastfeeding rates, not smoking, reducing alcohol intake, losing weight if obese, more education about prevention, monitoring, and treatment of illness, and stricter disease testing and quarantining in airports [28-50][91-93].

People claim that an unvaccinated child is a risk to their child, but they ignore the fact that their child is statistically more likely to be infected by themselves or a member of their own immediate family [94]. 

They ignore the fact that many vaccines don’t stop infection, they only reduce symptoms, making vaccine recipients silent disease carriers [95]. They ignore the fact that their vaccinated child poses a threat to those around them when their child receives live vaccines that can shed and replicate to full strength, causing disease epidemics instead of preventing them [95].

People claim disease epidemics have returned because of low vaccination rates, but they ignore the fact that vaccination rates are at an all time high and have remained stable over the last decade [96-97]. 

The logic is lost on them, or wilfully ignored. Any increased rates of disease obviously have little to do with the tiny percentage of people who don’t vaccinate, and everything to do with vaccine failure.

People tell us they were vaccinated as children and they’re ‘fine’ as if it’s proof vaccines are safe, but they scoff when someone else says they had a disease we vaccinate for as a child and they’re ‘fine’ too. 

Often people ignore the fact they were likely injected with half the amount of vaccines that children are injected with today; their childhood experience with vaccines is not an appropriate comparison to the vaccine schedule today [98-99]. They also ignore the fact that a lot of us aren’t ‘fine’. In the US 1 in 6 people now suffer from autoimmune disease [100], 1 in 5 children have a developmental and/or behavioral disability [101], and 1 in 42 boys have autism [102] – all of which are documented as adverse reactions to vaccination . That’s NOT a great definition of ‘fine’.

People claim that children are  no longer exposed to mercury from vaccines, but they ignore the fact that pregnant mothers are now recommended flu shots containing mercury [103], inadvertently exposing fetuses who are the most susceptible to mercury toxicity of any population. 

Additionally, childhood vaccines that are supposed to contain no mercury have tested positive for mercury contamination [104]. They ignore the fact that multiple vaccines containing the neurotoxin aluminium have been added to the childhood schedule, with levels grossly exceeding EPA guidelines [105-106]. Meaning the risk of neurological injury that was once posed by mercury laden vaccines, has now been replaced by aluminium laden vaccines.

I could keep going, it doesn’t end there. Jessica over at the Gianelloni Family blog has written an excellent piece called ‘Dear parents, you are being lied to’ that I also recommend reading:
http://gianelloni.wordpress.com/2014/04/07/dear-parents-you-are-being-lied-to/

Bottom line: don’t take anything at face value. If someone makes a statement about vaccines verify it by researching the studies to prove it, or disprove it – whatever the evidence ends up being. I wish I could say that after years of research I knew all the answers and that I felt at least something in this debate was proven 100%. But sadly the research that desperately needs to be done just hasn’t been done.

Unless we fiercely demand that the required research be done (ie. independent non-vax vs vax studies), it's likely no government agency will ever do it of their own accord. It’s up to us to bring it to the forefront of the media, the public, and our politicians.


References:

1.Blog Bullies & Hate Messages

2.The Dirty, Filthy Unvaccinated

3.Bombshell TV Show About HPV Vaccines Reveals Cruel Nature of Vaccine Pushers

4.Disease Risk: Measles

5.Disease Risk: Mumps

6.Disease Risk: Rubella

7.Disease Risk: Pertussis

8.Disease Risk: Rotovirus

9.Disease Risk: Hib meningitis

10.Disease Risk: Pneumococcal disease

11.Disease Risk: Influenza

12.Disease Risk: Varicella

13.Disease Risk: Tetanus

14.Disease Risk: Polio

15.Disease Risk: Hepatitis A

16.Disease Risk: Hepatitis B

17.Disease Risk: Diphtheria

18.Risk-Benefit Analysis: Measles, Mumps and Rubella

19.Risk-Benefit Analysis: Pneumoccocal, HPV, Meningococcal

20.Risk-Benefit Analysis: Diphtheria, Pertussis, and Tetanus

21.Risk-Benefit Analysis: Chicken Pox, Hib, Flu

22.Risk-Benefit Analysis: Hep A, Hep B, Rotavirus

23.Lioness Arising Mother Series

24.Parents Voice:  Children’s Adverse Outcomes Following Vaccination (huge list)

25.Stories of vaccine-injured children (huge list)
Raising a Sensitive Child

26.My child's vaccine reaction

27.The Childhood Immunization Schedule and Safety: Stakeholder Concerns, Scientific Evidence and Future Studies. Institute of Medicine Committee on the Assessment of Studies of Health Outcomes Related to the Recommended Childhood Immunization Schedule. Washington, DC: The National Academies Press 2013. pg 11
“The committee found that evidence assessing outcomes in subpopulations of children, who may be potentially susceptible to adverse reactions to vaccines (such as children with a family history of autoimmune disease or allergies or children born prematurely), was limited and is characterized by uncertainty about the definition of populations of interest and definitions of exposures or outcomes.”

28.How to boost your immune system

29.Vit C studies. Vitamin C function and status in chronic disease.
Nutrition in clinical care : an official publication of Tufts University.

30.Vitamin C and human health--a review of recent data relevant to human requirements.
International journal for vitamin and nutrition research.

31.Toward a new recommended dietary allowance for vitamin C based on antioxidant and health effects in humans. The American Journal of Clinical Nutrition

32.Randomized trial of vitamin D supplementation to prevent seasonal influenza A in schoolchildren
American Journal of Clinical Nutrition

33.Ample evidence exists from human studies that vitamin D reduces the risk of selected bacterial and viral infections. Experimental Biology and Medicine

34.Vitamin D-Mediated Induction of Innate Immunity in Gingival Epithelial Cells▿
Journal of Infection and Immunity

35.1,25-Dihydroxyvitamin D3 Treatment Shrinks Uterine Leiomyoma Tumors in the Eker Rat Model. Journal of Biology of Reproduction

36.Prevalence of eczema and food allergy is associated with latitude in Australia.
Journal of Allergy and Clinical Immunology

37.The Global Burden of Disease study and applications in water, sanitation and hygiene
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38.Estimating the burden of disease from water, sanitation, and hygiene at a global level.
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39.Sickness behavior induced by endotoxin can be mitigated by the dietary soluble fiber, pectin, through up-regulation of IL-4 and Th2 polarization. Journal of Brain, Behavior, and Immunity

40.Does tomato consumption effectively increase the resistance of lymphocyte DNA to oxidative damage? The American Journal of Clinical Nutrition

41.DNA damage and repair activity after broccoli intake in young healthy smokers
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42.Watercress supplementation in diet reduces lymphocyte DNA damage and alters blood antioxidant status in healthy adults. American Journal of Clinical Nutrition

43.A randomized trial of isonitrogenous enteral diets after severe trauma. An immune-enhancing diet reduces septic complications. Annals of Surgery

44.Upper respiratory tract infection is reduced in physically fit and active adults
British Journal of Sports Medicine

45.Risks of Formula Feeding
Natural Mama NZ

46.People at High Risk of Developing Flu–Related Complications
Centers for Disease Control and Prevention , September 9, 2014
"Children younger than 5, but especially children younger than 2 years old, Adults 65 years of age and older, Pregnant women, American Indians and Alaskan Natives, People who have medical conditions including: Asthma, Neurological and neurodevelopmental conditions [including disorders of the brain, spinal cord, peripheral nerve, and muscle such as cerebral palsy, epilepsy (seizure disorders), stroke, intellectual disability (mental retardation), moderate to severe developmental delay, muscular dystrophy, or spinal cord injury, Chronic lung disease (such as chronic obstructive pulmonary disease [COPD] and cystic fibrosis), Heart disease (such as congenital heart disease, congestive heart failure and coronary artery disease), Blood disorders (such as sickle cell disease), Endocrine disorders (such as diabetes mellitus), Kidney disorders, Liver disorders, Metabolic disorders (such as inherited metabolic disorders and mitochondrial disorders), Weakened immune system due to disease or medication (such as people with HIV or AIDS, or cancer, or those on chronic steroids), People younger than 19 years of age who are receiving long-term aspirin therapy, People who are morbidly obese (Body Mass Index, or BMI, of 40 or greater)."

47.Risk factors for community-acquired pneumonia diagnosed by general practitioners in the community. Farr BM1, et al. Respir Med. 2000 May;94(5):422-7. PMID: 10868703
“…these data suggest that cigarette smoking is the main avoidable risk factor for community-acquired pneumonia in adults.”

48.Alcohol consumption as a risk factor for pneumonia: a systematic review and meta-analysis.
Samokhvalov AV1, Irving HM, Rehm J. Epidemiol Infect. 2010 Dec;138(12):1789-95. PMID: 20380771. http://www.ncbi.nlm.nih.gov/pubmed/20380771
“…alcohol was found to be a risk factor for pneumonia with a clear statistical association, and a monotonic dose-response relationship.”

49.Who Is at Risk for Pneumonia? National Heart, Blood, and Lung Institute.
http://www.nhlbi.nih.gov/health/health-topics/topics/pnu/atrisk.html
“Your risk (of Pneumonia) also goes up if… you're exposed to certain chemicals, pollutants, or toxic fumes.”

50.Psychosocial factors and susceptibility to or outcome of acute respiratory tract infections.
Falagas ME et al. Int J Tuberc Lung Dis. 2010 Feb;14(2):141-8. PMID: 20074403
“Most of the relevant studies show a significant relationship between psychosocial factors and the onset or progression of acute respiratory tract illness.”

51.The reporting sensitivities of two passive surveillance systems for vaccine adverse events.
Rosenthal & Chen. Am J Public Health 1995; 85: pp. 1706-9.
http://www.ajph.org/cgi/reprint/85/12/1706?view=long&pmid=7503351
VAERS reports are estimated to be anywhere from less than 1% to 72% of the actual number of adverse events that occur; less than 1% for thrombocytopenia and rash after MMR, 4% for hypotonic-hyporesponsive episodes and 42% for seizures after DTP, 23% for seizures after MMR + MR, and 72% for vaccine-associated polio after OPV. Only 6 vaccine reactions were analysed, there was no analysis for autism or developmental delays.

52.MENINGITIS AND ENCEPHALITIS
JAMES F. BALE JR, MD. Current Management in Child Neurology, Third Edition 2005
“Young infants with encephalitis often have nonspecific signs, such as inactivity, poor feeding, irritability, “fussy” behavior, and “high-pitched” cries.”

53.Encephalitis. National Institutes of Health
“Symptoms in newborns and younger infants may not be as easy to recognize:… Irritability and crying more often (these symptoms may get worse when the baby is picked up)… If brain function is severely affected, interventions like physical therapy and speech therapy may be needed after the illness is controlled… The outcome varies. Some cases are mild and short, and the person fully recovers. Other cases are severe, and permanent impairment or death is possible. Permanent brain damage may occur in severe cases of encephalitis. It can affect:  Hearing, Memory, Muscle control, Sensation, Speech, and Vision.”

54.Effects Of Encephalitis. The Encephalitis Society

55.The Childhood Immunization Schedule and Safety: Stakeholder Concerns, Scientific Evidence and Future Studies. Institute of Medicine Committee on the Assessment of Studies of Health Outcomes Related to the Recommended Childhood Immunization Schedule. Washington, DC: The National Academies Press 2013. pg 11
http://books.nap.edu/openbook.php?record_id=13563&page=11
“Although each new vaccine is evaluated in the context of the overall immunization schedule that existed at the time of review of that vaccine, elements of the schedule are not evaluated once it is adjusted to accommodate a new vaccine. Thus, key elements of the entire schedule—the number, frequency, timing, order, and age at administration of vaccines—have not been systematically examined in research studies.”

56.Cal-Oregon Unvaccinated Survey. Generation Rescue, June 26, 2007

57.A Case Series of Children with Apparent Mercury Toxic Encephalopathies Manifesting with Clinical Symptoms of Regressive Autistic Disorders. D A Geier et al. J Toxicol Environ Health A. 2007 May 15;70(10):837-51. http://www.bhare.org/Geier2.pdf

58.A comprehensive review of mercury provoked autism. D.A. Geier et al. Indian J Med Res 128, October 2008, pp 383-411 http://www.icmr.nic.in/ijmr/2008/october/1004.pdf

59.A possible Central Mechanism in Autism Spectrum disorders, Part 1,2 & 3. Russell L Blaylock. Altern Ther Health Med. 2008 Nov-Dec;14(6):46-53. http://www.mpwhi.com/autism_part_1.pdf 

60.Abnormal measles-mumps-rubella antibodies and CNS autoimmunity in children with autism.
Singh VK et al. J Biomed Sci. 2002 Jul-Aug;9(4):359-64. PMID: 12145534
http://www.ncbi.nlm.nih.gov/pubmed/12145534

61.Acetaminophen (paracetamol) use, measles-mumps-rubella vaccination, and autistic disorder: the results of a parent survey.
 Schultz ST, et al. Autism. 2008 May;12(3):293-307.

62.Administration of aluminium to neonatal mice in vaccine-relevant amounts is associated with adverse long term neurological outcomes. Shaw CA, et al. J Inorg Biochem. 2013 Jul 19. pii: S0162-0134(13)00177-3.
http://www.ncbi.nlm.nih.gov/pubmed/23932735

63.Aluminum in the central nervous system (CNS): toxicity in humans and animals, vaccine adjuvants, and autoimmunity. Shaw CA, et al. Immunol Res. 2013 Jul;56(2-3):304-16. http://link.springer.com/article/10.1007%2Fs12026-013-8403-1

64.Autism: a novel form of mercury poisoning.
Sallie Bernard et al. Medical Hypotheses (2001) 56(4), 462–471

65.Case Control Study of Mercury Burden in Children with Autism Spectrum Disorder. James Adams, PhD [Arizona State University]. Journal of American Physicians and Surgeon, 2003. http://www.progressiveconvergence.com/A%20Case-Control%20Study%20of%20Mercury%20Burden%20in%20Children%20with%20Autistic%20Spectrum%20Disorders.pdf

66.Cultured lymphocytes from autistic children and non-autistic siblings up-regulate heat shock protein RNA in response to thimerosal challenge. Neurotoxicology. 2006 Sep;27(5):685-92. Walker SJ, Segal J, Aschner M. http://www.genome-explorations.com/images/pdfs_publications/10-Cultured%20lymphocytes%20from%20autistic%20children%20and%20non-autis.pdf

67.Detection and Sequencing of Measles Virus from Peripheral Mononuclear Cells from Patients with Inflammatory Bowel Disease and Autism. HISASHI KAWASHIMA et al. Digestive Diseases and Sciences, Vol. 45, No. 4 (April 2000), pp. 723–729 http://link.springer.com/article/10.1023%2FA%3A1005443726670#page-1

68.Detection of Measles Virus Genomic RNA in Cerebrospinal Fluid of Three Children with Regressive Autism: a Report of Three Cases. J.J. Bradstreet et al. J Am Physicians & Surgeons Vol 9 no.2 2004.
http://icdrc.org/documents/bradstreet.pdf

69.Do aluminum vaccine adjuvants contribute to the rising prevalence of autism?
Lucija Tomljenovic et al. J Inorganic Biochemistry Vol 105, Issue 11, 2011, Pg 1489–1499
http://www.ncbi.nlm.nih.gov/pubmed/22099159

70.Elevated levels of measles antibodies in children with autism. Singh VK, Jensen RL. Pediatr Neurol. 2003 Apr;28(4):292-4. http://www.ncbi.nlm.nih.gov/pubmed/12849883

71.Empirical Data Confirm Autism Symptoms Related to Aluminum and Acetaminophen Exposure. Stephanie Seneff, et al. Entropy, November 7, 2012

72.Hypothesis: conjugate vaccines may predispose children to autism spectrum disorders.

73.Influence of pediatric vaccines on amygdala growth and opioid ligand binding in rhesus macaque infants: A pilot study. Hewitson L t al. Acta Neurobiol Exp (Wars). 2010;70(2):147-64.Author information http://www.ncbi.nlm.nih.gov/pubmed/20628439

74.Phenotypic expression of autoimmune autistic disorder (AAD): a major subset of autism. Singh VK. Ann Clin Psychiatry. 2009 Jul-Sep;21(3):148-61. Brain State International Research Center. http://www.ncbi.nlm.nih.gov/pubmed/19758536

75.Risk of neurological and renal impairment associated with thimerosal containing vaccines
Center for Disease Control (CDC)

76.Increased risk of developmental neurologic impairment after high exposure to thimerosal-containing vaccine in first month of life. Thomas M. Verstraeten, R. Davies, D. Gu, F DeStefano. Division of Epidemiology and Surveillance, Vaccine Safety and Development Branch, National Immunization Program, Centers for Disease Control and Prevention. 1999.

77.Hepatitis B Vaccination of Male Neonates and Autism. CM Gallagher, MS Goodman. Annals of Epidemiology , Vol. 19, No. 9 ABSTRACTS (ACE), September 2009: 651-680,  p. 659

78.Measles-mumps-rubella vaccination timing and autism among young african american boys: a reanalysis of CDC data. Hooker BS. Transl Neurodegener. 2014 Aug 8;3:16.

79.CDC Whistle-Blower Reveals Cover-up Of Vaccine & Autism Link Data
August 27, 2014 by Lisa Bloomquist.

80.Is Big Pharma Addicted To Fraud? Erika Kelton, 7/29/2013, Forbes.
“Glaxo is accused of using a Shanghai travel agency to funnel at least $489 million in bribes.”

81.Home Pharma Recent 6 ‘Big Pharma’ frauds China 6 August 2013 Analysis
By Sheetal Sukhija, China 6 August 2013
“Each year big pharma giants end up spending billions of dollars in paying for fraud, misrepresentation of data and other such corruption allegations leveled out against them. In the last three years, global pharma giants have paid fines to the tune of $11 billion for criminal wrongdoing, including withholding safety data and promoting drugs for use, beyond any licensed condition. While GlaxoSmithKline (GSK) paid $3 billion, the biggest fine ever after pleading guilty on three criminal counts in US, Novartis ended up paying $420 million and Pfizer paid $2.3 billion in related scandals. “

82.Scientists Sue Merck: allege fraud, mislabeling, and false certification of MMR vaccine.
Suzanne Humphries, MD,  JUNE 25, 2012
“This is the story of the MMR vaccine and two Merck scientists who filed a lawsuit in 2010 over Merck’s efforts to allegedly “defraud the United States through Merck’s ongoing scheme to sell the government a mumps vaccine that is mislabeled, misbranded, adulterated and falsely certified as having an efficacy rate that is significantly higher than it actually is.” Merck allegedly did this from 2000 onwards in order to maintain its exclusive license to sell the MMR vaccine and keep its monopoly of the US market.

83.Pharmaceutical Industry Criminal and Civil Penalties: An Update
Sammy Almashat, Sidney Wolfe, September 27, 2012
“A total of 74 additional settlements, totaling $10.2 billion in financial penalties, were reached between the federal and state governments and pharmaceutical manufacturers between November 2, 2010 and July 18, 2012, with the first half of 2012 alone already representing a record year for both federal ($5.0 billion) and state ($1.6 billion) financial recoveries. Since 1991, a total of 239 settlements, for $30.2 billion, have now been reached (through July 18, 2012) between federal and state governments and pharmaceutical companies.”

84.How Corporations Corrupt Science at the Public's Expense (2012)
Union of Concerned Scientists. February 2012

85.Harvard Scientists warn about Epidemic of Side Effects due to Corruption

86.Public misinformed about seal of approval from FDA

87.‘All Trials’: because no test should go unheralded

88.SafeMinds Authored Commentary, Critiques & Presentations

89.Studies critiqued by VACCINES AND AUTISM –WHAT DO EPIDEMIOLOGICAL STUDIES REALLY TELL US? Coalition for SAFE MINDS

90.Vaccines Did Not Save Us – 2 Centuries Of Official Statistics

90a.  VAERS FAQS
http://vaers.hhs.gov/about/faqs

91.Development of an infection screening system for entry inspection at airport quarantine stations using ear temperature, heart and respiration rates. Sun G, et al. Conf Proc IEEE Eng Med Biol Soc. 2013;2013:6716-9. PMID: 24111284.
http://www.ncbi.nlm.nih.gov/pubmed/24111284
“We tested the system on 13 influenza patients and 33 normal subjects. The sensitivity of the infection screening system in detecting influenza were 92.3%, which was higher than the sensitivity reported in our previous paper (88.0%) with average facial skin temperature.”

92.Development of a non-contact screening system for rapid medical inspection at a quarantine depot using a laser Doppler blood-flow meter, microwave radar and infrared thermography. Matsui T, et al. J Med Eng Technol. 2009;33(5):403-9. PMID: 19440915
“In order to conduct fast screening of passengers with infections such as severe acute respiratory syndrome (SARS) or pandemic influenza at a quarantine depot, we developed a non-contact screening system with a self-produced program to conduct a human screening within five seconds, via a linear discriminant function from non-contact derived variables, i.e. palmer pulse derived from a laser Doppler blood-flow meter, respiration rate determined by a 10-GHz microwave radar, and facial temperature measured by a thermography … The proposed system appears promising for future application in fast screening of infection at a quarantine depot.”

93.Epidemiological trends and the effect of airport fever screening on prevention of domestic dengue fever outbreaks in Taiwan, 1998-2007. Kuan MM et al. Int J Infect Dis. 2010 Aug;14(8):e693-7.
http://www.ncbi.nlm.nih.gov/pubmed/20656647
“Our results show that airport fever screening had a positive effect on partially blocking the local transmission of imported dengue cases.”

94.Infant Pertussis: Who Was the Source? Bisgard, Kristine M. et al. Ped Infectious Disease J: Nov 2004 - Vol 23, Iss 11, pp 985-989

95.The implausibility of vaccine-based herd immunity
Natural Mama N Z

96.National Immunization Survey (NIS) - Children (19-35 months)
CDC, September 2, 2014

97.Nationwide vaccination coverage among children age 19-35 months, 2002-2012
CDC, Morb. Mortal. Wkly.

98.CDC Mandatory Vaccine Schedule: 1983 vs 2014
Peaceful Parenting, Monday, January 17, 2011

99.The Development of the Immunization Schedule

100.Autoimmune Statistics
The American Autoimmune Related Diseases Association
“We at AARDA say that 50 million Americans suffer from autoimmune disease.” US population in 2014 is 317 million people, meaning that 1 in 6 people suffer from autoimmune disease, or about 15%.

101.Identification of Developmental-Behavioral Problems in Primary Care: A Systematic Review
R. Christopher Sheldrick et al. PEDIATRICS Vol. 128 No. 2 August 1, 2011 pp. 356 -363
“Estimates indicate that at least 1 in 5 children has a developmental and/or behavioral disability.”

102.Prevalence of Autism Spectrum Disorder Among Children Aged 8 Years — Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2010
Jon Baio. Surveillance Summaries March 28, 2014 / 63(SS02);1-21
http://www.cdc.gov/mmwr/preview/mmwrhtml/ss6302a1.htm?s_cid=ss6302a1_w
“Approximately one in 42 boys and one in 189 girls living in the ADDM Network communities were identified as having ASD.”

103.Influenza Vaccines — United States, 2014–15 Influenza Season
Table displaying  amount of mercury in each flu vaccine. Flu vaccines that mercury include Afluria, FluLaval, Fluvirin, and Fluzone.

104. Mercury in vaccines from the Australian childhood immunization program schedule.
Austin DW, et al. Toxicol Environ Health A. 2010;73(10):637-40. PMID: 20391108
"Eight vaccines administered to children under the age of 5 yr were assessed for Hg content via a DMA-80 direct mercury analyzer. Seven of the 8 vaccines contained no detectable levels of Hg (less than 1 ppb); however, 1 vaccine (Infanrix hexa) tested positive for mercury at 10 ppb. The result was confirmed and validated by retesting the original sample. Follow-up testing was conducted on three additional samples of Infanrix hexa (one from the same production lot and two from a different lot). All three tested positive for mercury (average of 9.7 ppb).... the results of this study reveal that inaccuracies exist in public health messages, professional communications, and official documentation regarding Hg content in at least one childhood vaccine."

105.Childhood Vaccination: Aluminum. Natural Mama NZ.

106A.S.P.E.N. Statement on Aluminum in Parenteral Nutrition Solutions
P. Charney, The American Society for Parenteral and Enteral Nutrition (ASPEN) Aluminum Task Force, Nutrition in Clinical Practice 19 (August 2004): 416-417

107.Dear parents, you are being lied to. Gianelloni Family. POSTED ON APRIL 7, 2014

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2 comments

  1. Outstanding! May I share this?

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  2. This is impeccably documented & very well written. I'd love to share it, though not without your permission.
    Our son was injured by the DPT, decades ago, before the internet age, so we were left to wonder what had happened.
    I'm so glad moms have these resources today.
    The Simpsonwood transcripts should be required reading for young moms to be. I know it would have saved our family a world of hurt.

    ReplyDelete